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Naftin

NDC 54766-772 · HUMAN PRESCRIPTION DRUG · GEL

Generic nameNaftifine Hydrochloride
Labeler / ManufacturerSebela Pharmaceuticals Inc.
Marketing categoryNew Drug Application (innovator) · App NDA204286
Dosage form / routeGEL · TOPICAL
Active ingredientsNAFTIFINE HYDROCHLORIDE (2 g/100g)
Marketing started20180301
Marketing ended20261031
Package count2

External sources

Source: openFDA. Public-domain (CC0).